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"51655-713-52" National Drug Code (NDC)
Carvedilol 30 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (51655-713-52)
(Northwind Pharmaceuticals)
NDC Code
51655-713-52
Package Description
30 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (51655-713-52)
Product NDC
51655-713
Product Type Name
HUMAN PRESCRIPTION DRUG
Proprietary Name
Carvedilol
Non-Proprietary Name
Carvedilol
Dosage Form
TABLET, FILM COATED
Usage
ORAL
Start Marketing Date
20210528
Marketing Category Name
ANDA
Application Number
ANDA078384
Manufacturer
Northwind Pharmaceuticals
Substance Name
CARVEDILOL
Strength
3.125
Strength Unit
mg/1
Pharmacy Classes
Adrenergic alpha-Antagonists [MoA], Adrenergic beta1-Antagonists [MoA], Adrenergic beta2-Antagonists [MoA], alpha-Adrenergic Blocker [EPC], beta-Adrenergic Blocker [EPC]
Find more :
http://www.hipaaspace.com/medical_billing/coding/national.drug.codes/51655-713-52